Faster access than browser!Similarities between Genetic disorder and Prenatal testing
Genetic disorder and Prenatal testing have 19 things in common (in Unionpedia): Abortion, Amniocentesis, Asthma, Cleft lip and cleft palate, Cystic fibrosis, Diabetes mellitus, DNA, Down syndrome, Genetic disorder, Hypertension, Medical ultrasound, Mendelian inheritance, Minimally invasive procedures, Muscular dystrophy, Mutation, Prenatal testing, Sickle cell disease, Spinal muscular atrophy, Tay–Sachs disease.
Abortion
Abortion is the ending of pregnancy by removing an embryo or fetus before it can survive outside the uterus.
Abortion and Genetic disorder · Abortion and Prenatal testing ·
Amniocentesis
Amniocentesis (also referred to as amniotic fluid test or AFT) is a medical procedure used in prenatal diagnosis of chromosomal abnormalities and fetal infections, and also for sex determination, in which a small amount of amniotic fluid, which contains fetal tissues, is sampled from the amniotic sac surrounding a developing fetus, and then the fetal DNA is examined for genetic abnormalities.
Amniocentesis and Genetic disorder · Amniocentesis and Prenatal testing ·
Asthma
Asthma is a common long-term inflammatory disease of the airways of the lungs.
Asthma and Genetic disorder · Asthma and Prenatal testing ·
Cleft lip and cleft palate
Cleft lip and cleft palate, also known as orofacial cleft, is a group of conditions that includes cleft lip (CL), cleft palate (CP), and both together (CLP).
Cleft lip and cleft palate and Genetic disorder · Cleft lip and cleft palate and Prenatal testing ·
Cystic fibrosis
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine.
Cystic fibrosis and Genetic disorder · Cystic fibrosis and Prenatal testing ·
Diabetes mellitus
Diabetes mellitus (DM), commonly referred to as diabetes, is a group of metabolic disorders in which there are high blood sugar levels over a prolonged period.
Diabetes mellitus and Genetic disorder · Diabetes mellitus and Prenatal testing ·
DNA
Deoxyribonucleic acid (DNA) is a thread-like chain of nucleotides carrying the genetic instructions used in the growth, development, functioning and reproduction of all known living organisms and many viruses.
DNA and Genetic disorder · DNA and Prenatal testing ·
Down syndrome
Down syndrome (DS or DNS), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21.
Down syndrome and Genetic disorder · Down syndrome and Prenatal testing ·
Genetic disorder
A genetic disorder is a genetic problem caused by one or more abnormalities in the genome.
Genetic disorder and Genetic disorder · Genetic disorder and Prenatal testing ·
Hypertension
Hypertension (HTN or HT), also known as high blood pressure (HBP), is a long-term medical condition in which the blood pressure in the arteries is persistently elevated.
Genetic disorder and Hypertension · Hypertension and Prenatal testing ·
Medical ultrasound
Medical ultrasound (also known as diagnostic sonography or ultrasonography) is a diagnostic imaging technique based on the application of ultrasound.
Genetic disorder and Medical ultrasound · Medical ultrasound and Prenatal testing ·
Mendelian inheritance
Mendelian inheritance is a type of biological inheritance that follows the laws originally proposed by Gregor Mendel in 1865 and 1866 and re-discovered in 1900.
Genetic disorder and Mendelian inheritance · Mendelian inheritance and Prenatal testing ·
Minimally invasive procedures
Minimally invasive procedures (also known as minimally invasive surgeries) encompass surgical techniques that limit the size of incisions needed and so lessen wound healing time, associated pain and risk of infection.
Genetic disorder and Minimally invasive procedures · Minimally invasive procedures and Prenatal testing ·
Muscular dystrophy
Muscular dystrophy (MD) is a group of muscle diseases that results in increasing weakening and breakdown of skeletal muscles over time.
Genetic disorder and Muscular dystrophy · Muscular dystrophy and Prenatal testing ·
Mutation
In biology, a mutation is the permanent alteration of the nucleotide sequence of the genome of an organism, virus, or extrachromosomal DNA or other genetic elements.
Genetic disorder and Mutation · Mutation and Prenatal testing ·
Prenatal testing
Prenatal testing consists of prenatal screening and prenatal diagnosis, which are aspects of prenatal care that focus on detecting problems with the pregnancy as early as possible.
Genetic disorder and Prenatal testing · Prenatal testing and Prenatal testing ·
Sickle cell disease
Sickle cell disease (SCD) is a group of blood disorders typically inherited from a person's parents.
Genetic disorder and Sickle cell disease · Prenatal testing and Sickle cell disease ·
Spinal muscular atrophy
Spinal muscular atrophy (SMA) is a rare neuromuscular disorder characterised by loss of motor neurons and progressive muscle wasting, often leading to early death.
Genetic disorder and Spinal muscular atrophy · Prenatal testing and Spinal muscular atrophy ·
Tay–Sachs disease
Tay–Sachs disease is a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord.
Genetic disorder and Tay–Sachs disease · Prenatal testing and Tay–Sachs disease ·
The list above answers the following questions
- What Genetic disorder and Prenatal testing have in common
- What are the similarities between Genetic disorder and Prenatal testing
Genetic disorder and Prenatal testing Comparison
Genetic disorder has 98 relations, while Prenatal testing has 133. As they have in common 19, the Jaccard index is 8.23% = 19 / (98 + 133).
References
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